Regulatory Affairs Lead - Medical Devices (FDA Class III)
RadNet
RadNet is seeking a Sr. Regulatory Affairs Principal in Somerville, Massachusetts, responsible for developing regulatory strategies and ensuring compliance for high risk medical products, including AI technologies. You will work with cross-functional teams and lead regulatory submissions, ensuring all products meet necessary requirements. This role requires extensive experience in regulatory affairs and strong knowledge of FDA regulations. It offers the opportunity to shape the regulatory framework for innovative medical devices, requiring both strategic input and technical expertise. #J-18808-Ljbffr RadNet
Vacancy posted 4 days ago
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